Scientist / Senior Scientist
AstraZeneca AB / Biomedicinjobb / Göteborg
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hela Sverige At AstraZeneca, we unlock the power of What Science Can Do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. Be part of the team where you are empowered to follow the science!
Pharmaceutical Sciences is accountable for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca's therapeutic areas.
Within Early Product Development and Manufacture (EPDM) in Gothenburg, Sweden, the manufacturing unit is accountable for delivering a vast portfolio of early investigational medicinal products. We have a wide range of manufacturing assets in three separate manufacturing facilities, supplying different types of clinical trial material to studies across the globe.
We are now looking for a skilled Scientist/Senior Scientist to join us at EPDM. The role will be located at our R&D site in Gothenburg, Sweden. With more than 3000 employees from over 70 different countries, our vibrant Gothenburg site is a truly inspiring place to work.
The role
Within the EPDM manufacturing unit, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities below will have a significant impact on the speed, quality and cost of the AZ development portfolio. We expect the successful candidate to:
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Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
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Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform transactions in material management systems.
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Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
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Rapidly develop strong competence within relevant process technologies and build credibility and ability to drive and secure product establishment, scale-up and clinical manufactures.
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Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
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Assess records and report manufacturing and validation data accurately according to GMP.
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Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
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Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.
Experience/requirements
MSc in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry is essential for this role.
We are looking for a scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, teamwork and delivery focus. There is both scope and an expectation to build the range of accountabilities over time, in line with personal development.
Strong verbal and documentation skills in English is a requirement. We expect you to have a keen interest to learn and operate complex manufacturing equipment and develop your expertise in pharmaceutical process technology. Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of cGMP is a merit for this role.
So, what's next?
Are you already imagining yourself joining us? Good, because we can't wait to hear from you!
For more information about the position, please contact hiring manager Frederika Bramer via
Frederika.Bramer@astrazeneca.com.
Welcome with your application (CV and cover letter) no later than 12th February.
We will review the applications continuously so please apply as soon as possible.
Additional information
Our Gothenburg site
Life in Gothenburg
Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2023-02-10
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-157298".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Kontakt AstraZeneca
maria.elmberg1@astrazeneca.com Jobbnummer 7365365
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